rs769920153 Rat Genome Database

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Variant: rs769920153 -  Homo sapiens

RGD ID: 28904486
RS ID: rs769920153
ClinVar ID: CV890296
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRAT  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 155,671,678
GRCh38 4 154,750,526
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004744.5:c.*1390G>A
NG_009110.1:g.11516G>A
NC_000004.12:g.154750526G>A
NC_000004.11:g.155671678G>A
More... 		01/12/2018 3 prime utr variant uncertain significance Tapetoretinal degeneration
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:LRAT
Accession:NM_004744
Location:3UTRS;EXON

Gene Symbol:LRAT
Accession:NM_001301645
Location:3UTRS;EXON

Gene Symbol:LRAT
Accession:XM_047416405
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001144497 CLINVAR
  RCV001144498 CLINVAR
dbSNP (RS) rs769920153 CLINVAR
MedGen C0035334 CLINVAR
  C2750063 CLINVAR
NCBI Gene LRAT CLINVAR
OMIM 268000 CLINVAR
  604863 CLINVAR
  613341 CLINVAR
SNOMED CT 28835009 CLINVAR